US5501817A - Process for stabilizing aqueous zeolite suspensions using a linear fatty alcohol polyglycol ether having a specific degree of ethoxylation - Google Patents
Process for stabilizing aqueous zeolite suspensions using a linear fatty alcohol polyglycol ether having a specific degree of ethoxylation Download PDFInfo
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- US5501817A US5501817A US08/284,594 US28459494A US5501817A US 5501817 A US5501817 A US 5501817A US 28459494 A US28459494 A US 28459494A US 5501817 A US5501817 A US 5501817A
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- 150000002191 fatty alcohols Chemical class 0.000 title claims abstract description 30
- 239000000725 suspension Substances 0.000 title claims abstract description 29
- 239000010457 zeolite Substances 0.000 title claims abstract description 28
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 title claims abstract description 22
- 229910021536 Zeolite Inorganic materials 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title claims abstract description 15
- 230000000087 stabilizing effect Effects 0.000 title claims abstract description 7
- 238000007046 ethoxylation reaction Methods 0.000 title description 7
- 229920000151 polyglycol Polymers 0.000 title description 5
- 239000010695 polyglycol Substances 0.000 title description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims abstract description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- 125000001931 aliphatic group Chemical group 0.000 claims abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims abstract 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 15
- 239000007900 aqueous suspension Substances 0.000 claims description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 5
- 239000000375 suspending agent Substances 0.000 claims 2
- 150000002170 ethers Chemical class 0.000 abstract description 16
- -1 poly(ethylene glycol) Polymers 0.000 abstract description 10
- 239000002002 slurry Substances 0.000 abstract 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 239000013049 sediment Substances 0.000 description 10
- 239000003381 stabilizer Substances 0.000 description 10
- 238000007711 solidification Methods 0.000 description 9
- 230000008023 solidification Effects 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- 229910052681 coesite Inorganic materials 0.000 description 5
- 229910052906 cristobalite Inorganic materials 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 229910052682 stishovite Inorganic materials 0.000 description 5
- 229910052905 tridymite Inorganic materials 0.000 description 5
- 238000003860 storage Methods 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- 235000019864 coconut oil Nutrition 0.000 description 3
- 239000003240 coconut oil Substances 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CFOQKXQWGLAKSK-KTKRTIGZSA-N (13Z)-docosen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCO CFOQKXQWGLAKSK-KTKRTIGZSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- DJYWKXYRGAMLRE-QXMHVHEDSA-N (z)-icos-9-en-1-ol Chemical compound CCCCCCCCCC\C=C/CCCCCCCCO DJYWKXYRGAMLRE-QXMHVHEDSA-N 0.000 description 1
- TVPWKOCQOFBNML-SEYXRHQNSA-N (z)-octadec-6-en-1-ol Chemical compound CCCCCCCCCCC\C=C/CCCCCO TVPWKOCQOFBNML-SEYXRHQNSA-N 0.000 description 1
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
- CFOQKXQWGLAKSK-UHFFFAOYSA-N 13-docosen-1-ol Natural products CCCCCCCCC=CCCCCCCCCCCCCO CFOQKXQWGLAKSK-UHFFFAOYSA-N 0.000 description 1
- 102000005701 Calcium-Binding Proteins Human genes 0.000 description 1
- 108010045403 Calcium-Binding Proteins Proteins 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- JYIBXUUINYLWLR-UHFFFAOYSA-N aluminum;calcium;potassium;silicon;sodium;trihydrate Chemical compound O.O.O.[Na].[Al].[Si].[K].[Ca] JYIBXUUINYLWLR-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910001603 clinoptilolite Inorganic materials 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229910052675 erionite Inorganic materials 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- ALSTYHKOOCGGFT-MDZDMXLPSA-N oleyl alcohol Chemical compound CCCCCCCC\C=C\CCCCCCCCO ALSTYHKOOCGGFT-MDZDMXLPSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- LBIYNOAMNIKVKF-FPLPWBNLSA-N palmitoleyl alcohol Chemical compound CCCCCC\C=C/CCCCCCCCO LBIYNOAMNIKVKF-FPLPWBNLSA-N 0.000 description 1
- LBIYNOAMNIKVKF-UHFFFAOYSA-N palmitoleyl alcohol Natural products CCCCCCC=CCCCCCCCCO LBIYNOAMNIKVKF-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/128—Aluminium silicates, e.g. zeolites
- C11D3/1286—Stabilised aqueous aluminosilicate suspensions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
Definitions
- This invention relates to a process for stabilizing aqueous zeolite suspensions by addition of selected fatty alcohol polyethylene glycol ethers.
- Zeolites more particularly those of the zeolite A type, have particular significance as builders in modern detergents and have largely displaced the polyphosphates used for decades. Their advantages lie not only in a high calcium binding capacity, but also and above all in their high ecotoxicological compatibility Tens. Surf. Det., 24, 322 (1987)!.
- zeolites are obtained in the form of aqueous suspensions which may either be stored and marketed as such or subjected to spray drying. Zeolites show extremely low solubility in water so that zeolite suspensions readily sediment. In the most favorable case, this leads to phase separation although, normally, considerable quantities of the solid sink to the bottom of the vessels in storage, solidify and have to be removed, size-reduced and resuspended with considerable effort. In other cases, the suspension undergoes such a drastic increase in viscosity that transfer to other vessels or circulation by pumping becomes difficult, if not impossible, and always involves considerable product losses.
- German patent application DE 33 30 220 A1 it is proposed in German patent application DE 33 30 220 A1 to add 0.5 to 5% by weight of a mixture of fatty alcohol ethoxylates and fatty alcohol sulfates or fatty alcohol ether sulfates to the suspensions.
- German patent application DE 34 08 040 A1 describes a process for stabilizing 65% by weight zeolite A suspensions with 0.01 to 0.25% by weight of xanthan gum and carboxyl- or hydroxyl-containing polymers.
- zeolite suspensions can also be stabilized by addition of polyglycol ethers, fatty alcohol ether sulfates, fatty acid alkanolamides or fatty acid monoglycerides at pH 9 to 10.
- the problem addressed by the present invention was to provide an improved process for stabilizing aqueous zeolite suspensions which would be free from the described disadvantages.
- the present invention relates to a process for stabilizing aqueous zeolite suspensions by addition of surfactants, characterized in that fatty alcohol polyethylene glycol ethers corresponding to formula (I):
- R 1 is an aliphatic alkyl or alkenyl radical containing 12 to 18 carbon atoms and
- n is a number of 4 to 7
- zeolites are optionally water-containing alkali metal or alkaline earth metal alumosilicates corresponding to general formula (V):
- M is an alkali metal or alkaline earth metal with a valency of z
- x is a number of 1.8 to 12
- y is a number of 0 to 8 Chem. i. u. Zt., 20, 117 (1986)!.
- zeolites of which aqueous dispersions may be stabilized by the process according to the invention are the naturally occurring minerals clinoptilolite, erionite or chabasite.
- synthetic zeolites for example
- the aqueous suspensions may contain the zeolites in quantities of 20 to 60% by weight and preferably in quantities of 25 to 50% by weight.
- Fatty alcohol polyethylene glycol ethers are known nonionic surfactants which may be produced on an industrial scale by the ethoxylation process known per se.
- Stabilizers suitable for the process according to the invention are adducts of on average 4 to 7 moles of ethylene oxide with technical fatty alcohols containing 12 to 18 carbon atoms and 0 or 1 double bond.
- Typical examples are ethylene oxide adducts with lauryl alcohol, myristyl alcohol, cetyl alcohol, palmitoleyl alcohol, stearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, arachidyl alcohol, gadoleyl alcohol, behenyl alcohol and erucyl alcohol.
- the fatty alcohol polyethylene glycol ethers may have a conventional homolog distribution and also a narrow-range homolog distribution as obtained, for example, when the ethoxylation of the fatty alcohols is carried out in the presence of hydrotalcite catalysts.
- fatty alcohol polyethylene glycol ethers which are not derived from the pure alcohols, but instead from the technical cuts obtained for example in the selective hydrogenation of fatty acid methyl ester fractions based on vegetable or animal raw materials may also be used.
- Fatty alcohol polyethylene glycol ethers based on coconut oil fatty alcohols are preferably used.
- An adduct of on average 4.4 moles of ethylene oxide with a technical C 12/14 fatty alcohol and an adduct of on average 5 to 7 moles of ethylene oxide with a technical C 12/18 fatty alcohol having an iodine value of 5 to 95 and preferably 10 to 55 are particularly preferred.
- the fatty alcohol polyethylene glycol ethers may be used individually or even in the form of mixtures with one another. More particularly, it is even possible to use mixtures of fatty alcohol polyethylene glycol ethers having a relatively high and/or relatively low average degree of ethoxylation providing the average degree of ethoxylation of the resulting mixture lies within the range according to the invention of 4 to 5.
- the introduction of the fatty alcohol polyethylene glycol ethers into the suspension is not critical and may be carried out, for example, mechanically by stirring, optionally at elevated temperatures of 50° C. No chemical reaction takes place.
- the stabilizers may be added to the suspensions in quantities of 0.1 to 5% by weight and preferably in quantities of 1 to 3% by weight, based on the suspension.
- the zeolite suspensions obtainable by the process according to the invention are thermally stable and stable in storage. They are suitable, for example, for the production of detergent concentrates.
- A1 Adduct of on average 4.4 moles of ethylene oxide (EO) with a C 12-14 fatty alcohol Adduct of on average 4.4 moles of ethylene oxide (EO) with a C 12-14 fatty alcohol.
- Stabilizers A1 to A3 correspond to the invention while stabilizers B1 to B3 are comparison stabilizers.
- zeolite A zeolitic zeolitic microporous aqueous suspension of zeolite A (Sasil®, solids content: 49.6% by weight, free alkali content: 0.32% by weight, a product of Henkel KGaA, Du/ sseldorf, FRG) was introduced into a 500 ml glass beaker and quantities of 1.5% by weight, based on the suspension, of the stabilizers or stabilizer mixtures (expressed as solids) were then added.
- zeolite A Sud®, solids content: 49.6% by weight, free alkali content: 0.32% by weight, a product of Henkel KGaA, Du/ sseldorf, FRG
- the stability of the suspensions was measured over a period of 1 to 6 days at a temperature T of 20° to 50° C.
- the Brookfield viscosity and sedimentation behavior were determined using the following scale:
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A method for stabilizing aqueous zeolite suspensions by adding fatty-alcohol poly(ethylene glycol) ethers of the formula R1 O--(CH2 CH2 O)n in which R1 is a linear aliphatic alkyl group containing 12 to 14 carbon atoms and n is an average number of from 4.2 to 4.8. Aqueous slurries containing from 20 to 60% by weight of zeolite are stabilized by adding it to the slurry from 0.1 to 5% by weight of the fatty-alcohol poly(ethylene glycol) ethers.
Description
This invention relates to a process for stabilizing aqueous zeolite suspensions by addition of selected fatty alcohol polyethylene glycol ethers.
Zeolites, more particularly those of the zeolite A type, have particular significance as builders in modern detergents and have largely displaced the polyphosphates used for decades. Their advantages lie not only in a high calcium binding capacity, but also and above all in their high ecotoxicological compatibility Tens. Surf. Det., 24, 322 (1987)!.
In their production, zeolites are obtained in the form of aqueous suspensions which may either be stored and marketed as such or subjected to spray drying. Zeolites show extremely low solubility in water so that zeolite suspensions readily sediment. In the most favorable case, this leads to phase separation although, normally, considerable quantities of the solid sink to the bottom of the vessels in storage, solidify and have to be removed, size-reduced and resuspended with considerable effort. In other cases, the suspension undergoes such a drastic increase in viscosity that transfer to other vessels or circulation by pumping becomes difficult, if not impossible, and always involves considerable product losses.
There has been no shortage of attempts in the past to stabilize aqueous zeolite suspensions in such a way that they remain stable in storage for a sufficient time and can be transported through pipelines without blocking them.
For example, it is proposed in German patent application DE 33 30 220 A1 to add 0.5 to 5% by weight of a mixture of fatty alcohol ethoxylates and fatty alcohol sulfates or fatty alcohol ether sulfates to the suspensions.
German patent application DE 34 08 040 A1 describes a process for stabilizing 65% by weight zeolite A suspensions with 0.01 to 0.25% by weight of xanthan gum and carboxyl- or hydroxyl-containing polymers.
According to the teaching of German patent application DE 34 23 351 A1, zeolite suspensions can also be stabilized by addition of polyglycol ethers, fatty alcohol ether sulfates, fatty acid alkanolamides or fatty acid monoglycerides at pH 9 to 10.
In addition, the use of many other stabilizers, for example polycarboxylates having molecular weights above 1,500, phosphonic acids, phosphoric acid esters, alkyl benzenesulfonates, layer silicates DE-OS 25 27 388!, alkylphenol polyglycol ethers DE 34 01 861 A1!, isotridecyl polyglycol ethers DE 34 44 311 A1! and adducts of ethylene oxide with oxoalcohols DE 37 19 042 A1!, is known from the literature.
Unfortunately, known processes have disadvantages in regard to adequate stabilization over a relatively wide temperature range, in regard to the necessary quantities of stabilizer and also in regard to the viscosity and residue-free pouring behavior of the suspensions.
Accordingly, the problem addressed by the present invention was to provide an improved process for stabilizing aqueous zeolite suspensions which would be free from the described disadvantages.
The present invention relates to a process for stabilizing aqueous zeolite suspensions by addition of surfactants, characterized in that fatty alcohol polyethylene glycol ethers corresponding to formula (I):
R.sup.1 O--(CH.sub.2 CH.sub.2 O).sub.n H (I)
in which
R1 is an aliphatic alkyl or alkenyl radical containing 12 to 18 carbon atoms and
n is a number of 4 to 7,
are added to the suspensions.
It has surprisingly been found that the use of the selected fatty alcohol polyethylene glycol ethers mentioned or mixtures thereof with one another can reliably stabilize suspensions of zeolites over a broad temperature range, more particularly from 10° to 60° C. The suspensions also show high stability in storage over prolonged periods, can be pumped through pipelines and can be readily poured out with only minimal product losses.
In the context of the invention, zeolites are optionally water-containing alkali metal or alkaline earth metal alumosilicates corresponding to general formula (V):
M.sub.2/z O . Al.sub.2 O.sub.3 . x SiO.sub.2 . y H.sub.2 O (V)
in which M is an alkali metal or alkaline earth metal with a valency of z, x is a number of 1.8 to 12 and y is a number of 0 to 8 Chem. i. u. Zt., 20, 117 (1986)!.
Typical examples of zeolites of which aqueous dispersions may be stabilized by the process according to the invention are the naturally occurring minerals clinoptilolite, erionite or chabasite. However, synthetic zeolites, for example
zeolite X Na86 (AlO2)86 (SiO2)106 ! . 264 H2 O
zeolite Y Na56 (AlO2)56 (SiO2)136 ! . 325 H2 O
zeolite L K9 AlO2)9 SiO2)27 ! . 22 H2 O
mordenite Na8.7 AlO2)8.7 (SiO2)39.3 ! . 24 H2 O
are preferred,
zeolite A Na12 (AlO2)12 (SiO2)12 ! . 27 H2 O
being particularly preferred.
The aqueous suspensions may contain the zeolites in quantities of 20 to 60% by weight and preferably in quantities of 25 to 50% by weight.
Fatty alcohol polyethylene glycol ethers are known nonionic surfactants which may be produced on an industrial scale by the ethoxylation process known per se.
Stabilizers suitable for the process according to the invention are adducts of on average 4 to 7 moles of ethylene oxide with technical fatty alcohols containing 12 to 18 carbon atoms and 0 or 1 double bond. Typical examples are ethylene oxide adducts with lauryl alcohol, myristyl alcohol, cetyl alcohol, palmitoleyl alcohol, stearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, arachidyl alcohol, gadoleyl alcohol, behenyl alcohol and erucyl alcohol.
Fatty alcohol polyglycol ethers corresponding to formula (I), in which R1 is an alkyl radical containing 12 to 18 and more particularly 12 to 14 carbon atoms and n is a number of 4 to 5 and more particularly a number of 4.2 to 4.8, are preferred. The fatty alcohol polyethylene glycol ethers may have a conventional homolog distribution and also a narrow-range homolog distribution as obtained, for example, when the ethoxylation of the fatty alcohols is carried out in the presence of hydrotalcite catalysts.
In addition, fatty alcohol polyethylene glycol ethers which are not derived from the pure alcohols, but instead from the technical cuts obtained for example in the selective hydrogenation of fatty acid methyl ester fractions based on vegetable or animal raw materials may also be used. Fatty alcohol polyethylene glycol ethers based on coconut oil fatty alcohols are preferably used. An adduct of on average 4.4 moles of ethylene oxide with a technical C12/14 fatty alcohol and an adduct of on average 5 to 7 moles of ethylene oxide with a technical C12/18 fatty alcohol having an iodine value of 5 to 95 and preferably 10 to 55 are particularly preferred.
The fatty alcohol polyethylene glycol ethers may be used individually or even in the form of mixtures with one another. More particularly, it is even possible to use mixtures of fatty alcohol polyethylene glycol ethers having a relatively high and/or relatively low average degree of ethoxylation providing the average degree of ethoxylation of the resulting mixture lies within the range according to the invention of 4 to 5.
The introduction of the fatty alcohol polyethylene glycol ethers into the suspension is not critical and may be carried out, for example, mechanically by stirring, optionally at elevated temperatures of 50° C. No chemical reaction takes place. The stabilizers may be added to the suspensions in quantities of 0.1 to 5% by weight and preferably in quantities of 1 to 3% by weight, based on the suspension.
The zeolite suspensions obtainable by the process according to the invention are thermally stable and stable in storage. They are suitable, for example, for the production of detergent concentrates.
The following Examples are intended to illustrate the invention without limiting is in any way.
A1 Adduct of on average 4.4 moles of ethylene oxide (EO) with a C12-14 fatty alcohol.
A2 Mixture of two C12/14 fatty alcohol ethoxylates: 53.8% by weight adduct of on average 4.1 moles of EO 46.2% by weight adduct of on average 4.75 moles of EO average degree of ethoxylation: 4.4
A3 Mixture of two C12/14 fatty alcohol ethoxylates: 53.3% by weight adduct of on average 3.7 moles EO 46.7% by weight adduct of on average 5.2 moles EO average degree of ethoxylation: 4.4
B1 Adduct of on average 6.5 moles of ethylene oxide (EO) with isotridecyl alcohol.
B2 Adduct of on average 5.2 moles of ethylene oxide (EO) with C12-14 coconut oil fatty alcohol (iodine value <2).
B3 Adduct of on average 3.7 moles of ethylene oxide (EO) with C12-14 coconut oil fatty alcohol (iodine value <2).
Stabilizers A1 to A3 correspond to the invention while stabilizers B1 to B3 are comparison stabilizers.
An aqueous suspension of zeolite A (Sasil®, solids content: 49.6% by weight, free alkali content: 0.32% by weight, a product of Henkel KGaA, Du/ sseldorf, FRG) was introduced into a 500 ml glass beaker and quantities of 1.5% by weight, based on the suspension, of the stabilizers or stabilizer mixtures (expressed as solids) were then added.
The stability of the suspensions was measured over a period of 1 to 6 days at a temperature T of 20° to 50° C. The Brookfield viscosity and sedimentation behavior were determined using the following scale:
1=slight sediment, no solidification
2=slight sediment, slight solidification
3=slight sediment, pronounced solidification
4=distinct sediment, no solidification
5=distinct sediment, slight solidification
6=distinct sediment, pronounced solidification
7=thick sediment, no solidification
8=thick sediment, slight solidification
9=thick sediment, pronounced solidification
The test results are set out in Table 1.
TABLE 1 ______________________________________ Sedimentation of zeolite suspensions T Viscosity (mPa · s) Sedimentation Ex. Stab. °C. 1d 6d 1d 6d ______________________________________ 1 A1 20 2,000 2,000 1 1 2 A1 50 2,000 2,000 1 2 3 A2 20 2,000 2,000 1 2 4 A2 50 2,000 2,000 1 1 5 A3 20 2,000 2,000 1 1 6 A3 50 2,000 2,000 2 4 C1 B1 20 40,000 40,000 1 2 C2 B2 20 40,000 40,000 8 8 C3 B3 20 2,000 2,000 1 1 C4 B3 50 2,000 40,000 3 8 ______________________________________
Claims (4)
1. A process for stabilizing an aqueous zeolite suspension, which comprises: adding to the suspension comprising from 20% to 60% by weight of zeolite, from 0.1 to 5% by weight of the suspension of a suspending agent consisting essentially of at least one fatty alcohol polyethylene glycol ether of the formula: R1 O--(CH2 CH2 O)n wherein R1 consists essentially of a linear aliphatic alkyl group containing 12-14 carbon atoms and n is an average number of 4.2 to 4.8 for the total amount of fatty alcohol polyethylene glycol ether suspending agent.
2. The process of claim 1, wherein the fatty alcohol polyethylene glycol ether is added to an aqueous suspension of zeolite A.
3. The process of claim 1, wherein from 1% to 3% by weight, based on the weight of the suspension, of the fatty alcohol polyethylene glycol ether is added to the suspension.
4. The process of claim 2, wherein from 1% to 3% by weight, based on the weight of the suspension, of the fatty alcohol polyethylene glycol ether is added to the suspension.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4203789A DE4203789A1 (en) | 1992-02-10 | 1992-02-10 | METHOD FOR STABILIZING AQUEOUS ZEOLITE SUSPENSIONS |
DE4203789.1 | 1992-02-10 | ||
PCT/EP1993/000227 WO1993016159A1 (en) | 1992-02-10 | 1993-02-01 | Method of stabilizing aqueous zeolite suspensions |
Publications (1)
Publication Number | Publication Date |
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US5501817A true US5501817A (en) | 1996-03-26 |
Family
ID=6451311
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/284,594 Expired - Fee Related US5501817A (en) | 1992-02-10 | 1993-02-01 | Process for stabilizing aqueous zeolite suspensions using a linear fatty alcohol polyglycol ether having a specific degree of ethoxylation |
Country Status (7)
Country | Link |
---|---|
US (1) | US5501817A (en) |
EP (1) | EP0626004B1 (en) |
JP (1) | JPH07503493A (en) |
KR (1) | KR950700398A (en) |
DE (2) | DE4203789A1 (en) |
ES (1) | ES2086940T3 (en) |
WO (1) | WO1993016159A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10022691B2 (en) | 2015-10-07 | 2018-07-17 | Elementis Specialties, Inc. | Wetting and anti-foaming agent |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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FR2872152B1 (en) * | 2004-06-24 | 2006-08-11 | Inst Francais Du Petrole | HIERARCHISED POROSITY MATERIAL COMPRISING SILICON |
FR2920758B1 (en) * | 2007-09-07 | 2009-11-13 | Inst Francais Du Petrole | CRYSTALLIZED MATERIAL WITH HIERARCHISED POROSITY AND COMPRISING SILICON |
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- 1993-02-01 ES ES93909530T patent/ES2086940T3/en not_active Expired - Lifetime
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10022691B2 (en) | 2015-10-07 | 2018-07-17 | Elementis Specialties, Inc. | Wetting and anti-foaming agent |
US11052361B2 (en) | 2015-10-07 | 2021-07-06 | Elementis Specialties, Inc. | Wetting and anti-foaming agent |
US11634643B2 (en) | 2015-10-07 | 2023-04-25 | Elementis Specialties, Inc. | Wetting and anti-foaming agent |
Also Published As
Publication number | Publication date |
---|---|
KR950700398A (en) | 1995-01-16 |
ES2086940T3 (en) | 1996-07-01 |
JPH07503493A (en) | 1995-04-13 |
EP0626004A1 (en) | 1994-11-30 |
DE59302613D1 (en) | 1996-06-20 |
DE4203789A1 (en) | 1993-08-12 |
EP0626004B1 (en) | 1996-05-15 |
WO1993016159A1 (en) | 1993-08-19 |
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